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MEGAFILL MH - Indonesia BPOM Medical Device Registration

MEGAFILL MH is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602911421. The device is manufactured by MEGADENTA DENTALPRODUKTE GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MANDALA MITRATAMA.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : B
MEGAFILL MH
Analysis ID: AKL 20602911421

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. MANDALA MITRATAMA

AR Address

Komplek Ruko Roxy Mas Blok C 2 No. 12 Jl. Hasyim Ashari 125

Registration Date

Dec 29, 2022

Expiry Date

Dec 07, 2027

Product Type

Prosthetic Dental Equipment

Tooth shade resin material.

Non Electromedic Non Sterile

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